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1.
Mireille Christophe Michel-Levy Michle Bourot-Denise 《Meteoritics & planetary science》1992,27(1):73-80
Abstract— The mineral compositions of 250 micrometeorites have been studied and olivines and low-calcium pyroxenes with crystals larger than 5 μm have been analyzed. While magnesium-rich grains dominate, the Fa content of olivine may reach 50% and the Fs content of pyroxene may reach 26%. The Ca and Mn of the olivine show no consistent trends with increasing Fe, but Cr shows a negative correlation. For low-Ca pyroxene, Al and Cr contents are generally higher than in pyroxenes of equilibrated chondrites but similar to those of highly unequilibrated chondrites. Calcium-bearing pyroxene, feldspar and chromite are rare in the micrometeorites which were selected because of their high Mg, Si, Fe and their low Ca and Al content. All these minerals are found as coarse-grained particles often with adhering iron-rich scoria or as clasts in fine-grained or scoriaceous micrometeorites. Apart from a few particles which could be the debris of ordinary chondrites, most micrometeorites probably come from a common source similar, but not identical to carbonaceous chondrites, as shown by their lower Ni and S content and their different oxygen isotopic composition assuming two measurements performed on olivine grains prove to be typical. 相似文献
2.
Abstract— Platinum group elements (PGE) enrichments are found in Fe-Ni blebs (<1 μm) in Al- and Cr-rich objects in the ordinary chondrites Ste. Marguerite, Forest Vale, Montferré. In Ste. Marguerite, high ZrO2 concentrations (baddeleyite) are also present in a chromite inclusion. Iridium enrichment in this material compared to its metal content is confirmed by INAA. The widespread occurrence of PGE in Al- and Cr-rich objects, mostly present in H-group chondrites of nearly equilibrated types, must be taken into account to understand their conditions of formation. 相似文献
3.
S. C. Trager Guy Worthey S. M. Faber Alan Dressler 《Monthly notices of the Royal Astronomical Society》2005,362(1):2-8
We present numerical investigations into the formation of massive stars from turbulent cores of density structure ρ∝ r −1.5 . The results of five hydrodynamical simulations are described, following the collapse of the core, fragmentation and the formation of small clusters of protostars. We generate two different initial turbulent velocity fields corresponding to power-law spectra P ∝ k −4 and P ∝ k −3.5 , and we apply two different initial core radii. Calculations are included for both completely isothermal collapse, and a non-isothermal equation of state above a critical density (10−14 g cm−3 ) . Our calculations reveal the preference of fragmentation over monolithic star formation in turbulent cores. Fragmentation was prevalent in all the isothermal cases. Although disc fragmentation was largely suppressed in the non-isothermal runs due to the small dynamic range between the initial density and the critical density, our results show that some fragmentation still persisted. This is inconsistent with previous suggestions that turbulent cores result in the formation of a single massive star. We conclude that turbulence cannot be measured as an isotropic pressure term. 相似文献
4.
Abstract Dahmani is a shocked LL6 fragmental breccia. According to the composition of the silicates (olivine Fa30,32.6, orthopyroxene Fs24.5–26.3) and of the metal (a 60% Ni taenite) it is one of the most oxidised known. 相似文献
5.
A coupled deterministic hydrological and water temperature model, CEQUEAU, was modified to include soil temperature and crown closure in its calculation of local advective terms in the heat budget. The modified model was than tested to verify its sensitivity to these modifications. An analysis of the heat budget of a small forested catchment in eastern Canada revealed that the advective term related to interflow plays a significant role in the daily water heat budget, providing on average 28% of the local advective budget (which also includes advective heat terms from surface runoff and groundwater) and nearly 14% of the total heat budget (which includes all radiative terms at the water surface, convection and evaporation, as well as the local advective terms). Relative sensitivity indices (RSIs) were used to verify the impact of the newly introduced parameters and variables. Among them, parameters related to the forest cover (crown closure and leaf area index) have a maximum RSI of ?0·6; i.e. a 100% increase in value produces a 60% decrease in the local advective term. Parameters with the greatest influence are the volume of water contributing to interflow and the amplitude of the net radiative flux at the soil surface, which, if doubled, would double the contribution of the local interflow advective term to the heat budget. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
6.
Eloïse Gaillou Aurlien Delaunay Benjamin Rondeau Martine Bouhnik-le-Coz Emmanuel Fritsch Guy Cornen Christophe Monnier 《Ore Geology Reviews》2008,34(1-2):113
Seventy-seven gem opals from ten countries were analyzed by inductively coupled plasma-mass spectrometry (ICP-MS) through a dilution process, in order to establish the nature of the impurities. The results are correlated to the mode of formation and physical properties and are instrumental in establishing the geographical origin of a gem opal. The geochemistry of an opal is shown to be dependant mostly on the host rock, at least for examples from Mexico and Brazil, even if modified by weathering processes. In order of decreasing concentration, the main impurities present are Al, Ca, Fe, K, Na, and Mg (more than 500 ppm). Other noticeable elements in lesser amounts are Ba, followed by Zr, Sr, Rb, U, and Pb. For the first time, geochemistry helps to discriminate some varieties of opals. The Ba content, as well as the chondrite-normalized REE pattern, are the keys to separating sedimentary opals (Ba > 110 ppm, Eu and Ce anomalies) from volcanic opals (Ba < 110 ppm, no Eu or Ce anomaly). The Ca content, and to a lesser extent that of Mg, Al, K and Nb, helps to distinguish gem opals from different volcanic environments. The limited range of concentrations for all elements in precious (play-of-color) compared to common opals, indicates that this variety must have very specific, or more restricted, conditions of formation. We tentatively interpreted the presence of impurities in terms of crystallochemistry, even if opal is a poorly crystallized or amorphous material. The main replacement is the substitution of Si4+ by Al3+ and Fe3+. The induced charge imbalance is compensated chiefly by Ca2+, Mg2+, Mn2+, Ba2+, K+, and Na+. In terms of origin of color, greater concentrations of iron induce darker colors (from yellow to “chocolate brown”). This element inhibits luminescence for concentrations above 1000 ppm, whereas already a low content in U (≤ 1 ppm) induces a green luminescence. 相似文献
7.
Geneviève Bordeleau Richard Martel Dirk Schäfer Guy Ampleman Sonia Thiboutot 《Environmental Geology》2008,55(2):385-396
Numerical modelling was done at the Cold Lake Air Weapons Range, Canada, to test whether the dissolved RDX and nitrate detected
in groundwater come from the same sources, and to predict whether contamination poses a threat to the surface water receptors
near the site. Military live fire training activities may indeed pose a risk of contamination to groundwater resources, however
field investigations on military bases are quite recent, and little information is available on the long-term behaviour of
munition residues related contaminants. Very limited information was available about the contaminant source zones, which were
assigned based on our knowledge of current training activities. The RDX plume was well represented with the model, but the
heterogeneous distribution of nitrate concentrations was more difficult to reproduce. It was nonetheless determined that both
contaminants originate from the same areas. According to the model, both contaminants should reach the nearby river, but concentrations
in the river should remain very low if the source zone concentration does not change. Finally, the model allowed the recommendation
of a new location for the main bombing target, which would offer added protection to the river and the lake into which it
flows. 相似文献
8.
Magnesium isotope systematics of the lithologically varied Moselle river basin, France 总被引:2,自引:0,他引:2
Agnès Brenot Christophe Cloquet Nathalie Vigier Jean Carignan Christian France-Lanord 《Geochimica et cosmochimica acta》2008,72(20):5070-5089
Magnesium and strontium isotope signatures were determined during different seasons for the main rivers of the Moselle basin, northeastern France. This small basin is remarkable for its well-constrained and varied lithology on a small distance scale, and this is reflected in river water Sr isotope compositions. Upstream, where the Moselle River drains silicate rocks of the Vosges mountains, waters are characterized by relatively high 87Sr/86Sr ratios (0.7128-0.7174). In contrast, downstream of the city of Epinal where the Moselle River flows through carbonates and evaporites of the Lorraine plateau, 87Sr/86Sr ratios are lower, down to 0.70824.Magnesium in river waters draining silicates is systematically depleted in heavy isotopes (δ26Mg values range from −1.2 to −0.7‰) relative to the value presently estimated for the continental crust and a local diorite (−0.5‰). In comparison, δ26Mg values measured in soil samples are higher (∼0.0‰). This suggests that Mg isotope fractionation occurs during mineral leaching and/or formation of secondary clay minerals. On the Lorraine plateau, tributaries draining marls, carbonates and evaporites are characterized by low Ca/Mg (1.5-3.2) and low Ca/Sr (80-400) when compared to local carbonate rocks (Ca/Mg = 29-59; Ca/Sr = 370-2200), similar to other rivers draining carbonates. The most likely cause of the Mg and Sr excesses in these rivers is early thermodynamic saturation of groundwater with calcite relative to magnesite and strontianite as groundwater chemistry progressively evolves in the aquifer. δ26Mg of the dissolved phases of tributaries draining mainly carbonates and evaporites are relatively low and constant throughout the year (from −1.4‰ to −1.6‰ and from −1.2‰ to −1.4‰, respectively), within the range defined for the underlying rocks. Downstream of Epinal, the compositions of the Moselle River samples in a δ26Mg vs. 87Sr/86Sr diagram can be explained by mixing curves between silicate, carbonate and evaporite waters, with a significant contribution from the Vosgian silicate lithologies (>70%). Temporal co-variation between δ26Mg and 87Sr/86Sr for the Moselle River throughout year is also observed, and is consistent with a higher contribution from the Vosges mountains in winter, in terms of runoff and dissolved element flux. Overall, this study shows that Mg isotopes measured in waters, rocks and soils, coupled with other tracers such as Sr isotopes, could be used to better constrain riverine Mg sources, particularly if analytical uncertainties in Mg isotope measurements can be improved in order to perform more precise quantifications. 相似文献
9.
Geochemical and hydrodynamic constraints on the distribution of trace metal concentrations in the lagoon of Nouméa, New Caledonia 总被引:1,自引:0,他引:1
Christophe Migon Sylvain Ouillon Xavier Mari Emmanuel Nicolas 《Estuarine, Coastal and Shelf Science》2007,74(4):756
Seawater samples were collected in the lagoon of Nouméa (southwest New Caledonia) along two transects from eutrophic coastal bays to the oligotrophic barrier reef. Land-based emissions to the lagoon were measured with dissolved and particulate concentrations of chromium (Cr) and nickel (Ni), used as tracers of both terrigenous and industrial (Ni ore treatment) activities, as well as dissolved and particulate concentrations of zinc (Zn), used as a tracer of urban effluents. The spatial variability of metal concentrations was related to geochemical and hydrodynamic conditions, i.e., respectively: (1) natural and anthropogenic emission sources, and chemical processes occurring in the water column; and (2) water residence times. The parameter used to describe the residence time of water masses was the local e-flushing time, i.e. the time required for a tracer mass contained within a given station to be reduced by a factor 1/e. High metal concentrations were found in coastal areas (up to 9000 ng dissolved Ni L−1), and steeply decreased with distance from the coast (down to 101 ng dissolved Ni L−1 near the barrier reef) to reach levels similar to those found in remote Pacific waters, suggesting a rapid renewal of waters close to the barrier. Distributions of metals in the lagoon are controlled upstream by land-based emission sources and later chemical processes. Then hydrodynamics constrain metal distributions, as shown by the observed relationship between local e-flushing times and the spatial variability of metal concentrations. In addition, a change in the direction of prevailing winds yielded a decrease of dissolved metal concentrations at the same site by a factor of 2.5 (Cr and Ni) and 2.9 (Zn). It is suggested that the residence time is a key parameter in the control of elemental concentrations in the lagoon waters, as much as land-based emission sources. 相似文献
10.
We present new sea-level data from the coasts of southern Tunisia, between the Gulf of Gabès and the Libyan border. The work tests, previously, published evidence on Holocene shorelines, and confirmed that a distinct emergence has occurred in this area during this time. The emergence peak lies at least 186 ± 11 cm above present and is inferred from: (1) AMS radiocarbon dates of subtidal vermetids and boring shells collected in growth position, and (2) careful assessment of tidal heights. Maximum emergence took place between about 6000 and 5000 14C years BP; it cannot be ascribed to tectonics and is probably related to post-glacial hydro-isostatic effects. It challenges the inference of a 3-m global sea-level rise since 6000 years BP due to residual Antarctic melting. 相似文献